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Noise induced bimodality in genetic circuits with monostable positive feedback

机译:噪声诱导在遗传电路中具有单稳态正反馈的遗传电路

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The expression of individual genes can be maintained through positive feedback loop mechanisms. If genes are expressed in bursts, then feedback either affects the frequency with which bursts occur or their size. Here we use a tractable hybrid modelling framework to evaluate how noncooperative positive feedback in burst frequency or burst size impacts the protein-level distribution. We confirm the results of previous studies that noncooperative positive feedback in burst frequency can support bimodal distributions. Intriguingly, bimodal distributions are unavailable in the case of feedback in burst size in the hybrid framework. However, kinetic Monte Carlo simulations of a full discrete model show that bimodality can reappear due to low-copy number effects. The two types of feedbacks lead to dramatically different values of protein mean and noise. We show that small values of leakage imply a small protein mean for feedback in burst frequency but not necessarily for feedback in burst size. We also show that protein noise decreases in response to gene activation if feedback is in burst frequency but there is a secondary noise amplification if feedback acts on burst size. Our results suggest that feedback in burst size and feedback in burst frequency may play fundamentally different roles in maintaining and controlling stochastic gene expression.
机译:通过正反馈回路机构可以保持单个基因的表达。如果基因以突发表示,则反馈会影响发生突发的频率或其尺寸。在这里,我们使用Trocrable混合建模框架来评估爆发频率或突发大小的非自由度阳性反馈会影响蛋白质水平分布。我们确认先前研究的结果,即爆发频率的非自由度正反馈可以支持双峰分布。有趣的是,在混合框架中的突发大小的反馈情况下,双模分布不可用。然而,全离散模型的动力学蒙特卡罗模拟表明,由于低拷贝数效应,双极性可以重新出现。两种类型的反馈导致蛋白质均值和噪声的显着不同。我们表明泄漏的小值意味着在突发频率的反馈中的小蛋白质意味着,但不一定用于突发大小的反馈。我们还表明,如果反馈处于突发频率,则蛋白质噪声响应于基因激活而降低,但如果反馈在突发大小作用,则存在次级噪声放大。我们的结果表明,在突发频率的突发​​大小和反馈中的反馈可能在维持和控制随机基因表达方面起着基本不同的作用。

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